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  5. NDC Package Code: 59726-834-14 Mucus Dm Extended-release

NDC Package 59726-834-14 Mucus Dm Extended-release

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
59726-834-14
Package Description:
14 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK
Product Code:
59726-834
Proprietary Name:
Mucus Dm Extended-release
Usage Information:
Do not crush, chew, or break tablet take with a full glass of water this product can be administered without regard for timing of mealsadults and children 12 years of age and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hourschildren under 12 years of age: do not use
11-Digit NDC Billing Format:
59726083414
NDC to RxNorm Crosswalk:
  • RxCUI: 1099074 - guaiFENesin 1200 MG / dextromethorphan HBr 60 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1099074 - 12 HR dextromethorphan hydrobromide 60 MG / guaifenesin 1200 MG Extended Release Oral Tablet
  • RxCUI: 1099074 - dextromethorphan hydrobromide 60 MG / guaifenesin 1200 MG 12 HR Extended Release Oral Tablet
    • Labeler Name:
    P & L Development, Llc
    Sample Package:
    No
    Start Marketing Date:
    01-01-2019
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59726-834-14?

    The NDC Packaged Code 59726-834-14 is assigned to a package of 14 blister pack in 1 carton / 1 tablet in 1 blister pack of Mucus Dm Extended-release, labeled by P & L Development, Llc. The product's dosage form is and is administered via form.

    Is NDC 59726-834 included in the NDC Directory?

    No, Mucus Dm Extended-release with product code 59726-834 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by P & L Development, Llc on January 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 59726-834-14?

    The 11-digit format is 59726083414. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-259726-834-145-4-259726-0834-14